MOF-derived bimetallic coordination polymer@cobalt-aluminum layered double hydroxide for highly selective CO2 adsorption: Experiments, mechanisms

Selective capture of CO2 is one of the most effective strategies for combating the greenhouse effect. In this study, we report the synthesis of a novel adsorbent-an amine-based cobalt-aluminum layered hydroxide with a hafnium/titanium metal coordination polymer (denoted as Co-Al-LDH@Hf/Ti-MCP-AS)-through the derivatization of metal-organic frameworks (MOFs) for selective CO2 adsorption and separation. Co-Al-LDH@Hf/Ti-MCP-AS achieved the maximum CO2 adsorption capacity of 2.57 mmol g(-1) at 25 degrees C and 0.1 MPa. The adsorption behavior followed the pseudo-second-order kinetics and Freundlich isotherm models, indicating that chemisorption occurs on a non-homogeneous surface. Co-Al-LDH@Hf/Ti-MCP-AS also exhibited selective CO2 adsorption in CO2/N-2 and excellent stability over six adsorption-desorption cycles. An in-depth analysis of the adsorption mechanism through X-ray photoelectron spectroscopy and density-functional theory and frontier molecular orbital calculations revealed that adsorption occurs through acid-base interactions between amine functional groups and CO2 and that the tertiary amines (N3) have the highest affinity toward CO2. Our study provides a novel strategy for designing high-performance adsorbents for CO2 adsorption and separation.

Automated summary

In this study, a novel adsorbent, Co-Al-LDH@Hf/Ti-MCP-AS, was synthesized for selective CO2 adsorption and separation. The maximum CO2 adsorption capacity of Co-Al-LDH@Hf/Ti-MCP-AS was 2.57 mmol g(-1) at 25 degrees C and 0.1 MPa. The adsorption behavior followed the pseudo-second-order kinetics and Freundlich isotherm models, and the adsorption occurred through acid-base interactions between amine functional groups and CO2.